Liou C H, Hsu H H, Hsueh C J, Juan C J, Chen C Y
Department of Radiology, Tri-Service General Hospital & National Defense Medical Center, Taipei, Taiwan.
J Formos Med Assoc. 2001 Oct;100(10):712-4.
Isolated intradiaphragmatic bronchogenic cysts are extremely rare. Here, we report a case of intradiaphragmatic bronchogenic cyst with calcifications in a 34-year-old man presenting with no clinical symptoms. Imaging studies of the chest, including chest roentgenogram and computerized tomography (CT), revealed a left posterior mediastinal mass that abutted onto the left diaphragmatic crus with multiple calcifications and showed no enhancement after contrast administration on CT. The patient underwent surgical resection of the mass. Intradiaphragmatic bronchogenic cyst with calcifications was diagnosed by pathology. The patient was discharged 10 days after the operation, and no complication was found 3 months later at follow-up.
孤立性膈内支气管源性囊肿极为罕见。在此,我们报告一例34岁男性膈内支气管源性囊肿伴钙化,该患者无临床症状。胸部影像学检查,包括胸部X线片和计算机断层扫描(CT),显示左后纵隔肿块,与左膈脚相邻,有多处钙化,CT增强扫描后无强化。患者接受了肿块的手术切除。病理诊断为膈内支气管源性囊肿伴钙化。患者术后10天出院,3个月后随访未发现并发症。